Cathode and lithium battery using the same
a lithium battery and cathode technology, applied in the direction of nickel compounds, cell components, sustainable manufacturing/processing, etc., can solve the problems of increasing structural instability, and achieve the effect of improving electrical characteristics
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example 1
Preparation of a Cathode Active Material
[0071]A cathode active material was synthesized by using the following combustion synthesis method. First, as a starting material, lithium carbonate, nickel acetate, cobalt acetate, manganese acetate, and lanthanum(III) nitrate hexahydrate were measured to satisfy the stoichiometry and were dissolved in 200 ml of a dilute nitric acid aqueous solution. Then, 15 ml of a citric acid aqueous solution and 15 ml of ethylene glycol were added to prepare a sol. The sol was stirred and heated on a hot plate to evaporate the water, and thus the mixture was obtained in a gel state. The gel heated on the hot plate until it was burned, and an additional heat treatment was performed after completely decomposing the gel by combustion. The additional heat treatment was performed at a temperature of 950° C. for 5 hours with a dry air flow, and thus a cathode active material powder of 0.5Li[La0.01Li0.32Mn0.67]O2-0.5LiNi1 / 3CO1 / 3Mn1 / 3O2, including the slightest q...
example 2
Preparation of a Cathode Active Material
[0076]A cathode active material was synthesized by using the following combustion synthesis method. First, as a starting material, lithium carbonate, nickel acetate, cobalt acetate, manganese acetate, and lanthanum(III) nitrate hexahydrate were measured to satisfy the stoichiometry and were dissolved in 200 ml of a dilute nitric acid aqueous solution. Then, 15 ml of a citric acid aqueous solution and 15 ml of ethylene glycol were added to prepare a sol. The sol was stirred and heated on a hot plate to evaporate the water, and thus the mixture was obtained in a gel state. Combustion of the gel was also performed on the hot plate, and an additional heat treatment was performed after completely decomposing the gel by combustion. The additional heat treatment was performed at a temperature of 950° C. for 5 hours with a dry air flow, and thus, a cathode active material powder of 0.5Li[La0.01Li0.32Mg0.02Mn0.65]O2-0.5LiNi1 / 3Co1 / 3Mn1 / 3O2, including th...
experimental example 1
Analysis of Crystalline Structure
[0081]FIG. 2 illustrates the results of the X-ray Diffraction (XRD) analysis of the cathode active materials obtained in the Comparative Example and Examples 1 and 2. From the XRD analysis of FIG. 2, the cathode active material of Example 1 had a secondary state which included LaNiO3. LaCoO3, and LaMnO3 of a perovskite structure. The cathode active material of Example 2 included LaNiO3, LaCoO3, LaMnO3, and LaMgO3 of a perovskite structure.
[0082]Peak positions of the LaNiO3, LaCoO3, LaMnO3, and LaMgO3 are as follows:
[0083]LaNiO3: 32.893 (110), 33.191 (012), 47.332 (202);
[0084]LaCoO3: 33.015 (110), 33.421 (104), 47.596 (024);
[0085]LaMnO3: 32.412 (112), 45.668 (220), 47.280 (221); and
[0086]LaMgO3: 32.608 (121), 32.702 (200), 46.740 (202).
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